z-logo
Premium
Photodynamic therapy for pythiosis
Author(s) -
Pires Layla,
Bosco Sandra de M. G.,
da Silva Junior Nelson F.,
Kurachi Cristina
Publication year - 2013
Publication title -
veterinary dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.744
H-Index - 60
eISSN - 1365-3164
pISSN - 0959-4493
DOI - 10.1111/j.1365-3164.2012.01112.x
Subject(s) - photodynamic therapy , in vivo , photosensitizer , amphotericin b , in vitro , porphyrin , microbiology and biotechnology , biology , pathology , medicine , chemistry , antifungal , biochemistry , organic chemistry
Background –  Pythiosis is a life‐threatening disease caused by Pythium insidiosum . Photodynamic therapy (PDT) is an alternative treatment to surgery that uses the interaction of a photosensitizer, light and molecular oxygen to cause cell death. Objectives –  To evaluate the effect of PDT on the in vitro growth of P. insidiosum and in an in vivo model of pythiosis. Methods –  For in vitro studies, two photosensitizers were evaluated: a haematoporphyrin derivative (Photogem ® ) and a chlorine (Photodithazine ® ). Amphotericin B was also evaluated, and the control group was treated with sterile saline solution. All experiments (PDT, porphyrin, chlorine and light alone, amphotericin B and saline solution) were performed as five replicates. For in vivo studies, six rabbits were inoculated with 20,000 zoospores of P. insidiosum , and an area of 1 cm 3 was treated using the same sensitizers. The PDT irradiation was performed using a laser emitting at 660 nm and a fluence of 200 J/cm 2 . Rabbits were clinically evaluated daily and histopathological analysis was performed 72 h after PDT. Results –  For in vitro assays, inhibition rates for PDT ranged from 60 to 100% and showed better results in comparison to amphotericin B. For the in vivo assays, after PDT, histological analysis of lesions showed a lack of infection up to 1 cm in depth. Conclusions and clinical importance –  In vitro and in vivo studies showed that PDT was effective in the inactivation of P. insidiosum and may represent a new approach to treating pythiosis.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom